Incidental Mutation 'R8048:Oas1f'
ID618869
Institutional Source Beutler Lab
Gene Symbol Oas1f
Ensembl Gene ENSMUSG00000053765
Gene Name2'-5' oligoadenylate synthetase 1F
Synonyms
Accession Numbers
Is this an essential gene? Probably non essential (E-score: 0.059) question?
Stock #R8048 (G1)
Quality Score225.009
Status Not validated
Chromosome5
Chromosomal Location120847367-120857986 bp(+) (GRCm38)
Type of Mutationmissense
DNA Base Change (assembly) G to T at 120847537 bp
ZygosityHeterozygous
Amino Acid Change Glycine to Valine at position 49 (G49V)
Ref Sequence ENSEMBL: ENSMUSP00000056993 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000057814]
Predicted Effect probably damaging
Transcript: ENSMUST00000057814
AA Change: G49V

PolyPhen 2 Score 1.000 (Sensitivity: 0.00; Specificity: 1.00)
SMART Domains Protein: ENSMUSP00000056993
Gene: ENSMUSG00000053765
AA Change: G49V

DomainStartEndE-ValueType
Pfam:OAS1_C 169 353 4.6e-81 PFAM
Predicted Effect probably benign
Transcript: ENSMUST00000123431
Coding Region Coverage
  • 1x: 100.0%
  • 3x: 99.9%
  • 10x: 99.7%
  • 20x: 98.9%
Validation Efficiency
Allele List at MGI
Other mutations in this stock
Total: 63 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Abcc1 A T 16: 14,410,844 L318F probably damaging Het
Alms1 T A 6: 85,641,334 S2318R probably benign Het
Arhgap12 G A 18: 6,052,883 T443I probably benign Het
Arhgap29 C T 3: 121,992,901 R372W probably damaging Het
Astn1 T C 1: 158,688,638 I1266T probably benign Het
Bsg T C 10: 79,709,746 V164A probably benign Het
C1qa G T 4: 136,896,610 S94R probably benign Het
Cadps2 A G 6: 23,838,863 V92A probably benign Het
Card6 TTGGGAGGACTGTGGATGAGAGGGCTTAGCATGGGAGGACTGTGGATGAGAGGGCTTAGCATGGGAGGACTGTGGATGAGAGGGCTTAGCATGGGAGGACTGCGGATGAGAGGGCTTAGCATGGGAGGACTG TTGGGAGGACTGTGGATGAGAGGGCTTAGCATGGGAGGACTGTGGATGAGAGGGCTTAGCATGGGAGGACTGCGGATGAGAGGGCTTAGCATGGGAGGACTG 15: 5,098,691 probably benign Het
Ccdc187 T A 2: 26,293,514 D158V possibly damaging Het
Cngb1 T A 8: 95,263,210 Y758F possibly damaging Het
Ddx4 G A 13: 112,622,172 A285V probably null Het
Dsg1c A T 18: 20,274,767 K390M probably damaging Het
Dst T C 1: 34,190,636 F2437L probably benign Het
Eln CTCCAGCTCCGAT C 5: 134,729,149 probably benign Het
Fam227a CATTGTCTTGA CA 15: 79,649,758 probably null Het
Fez2 T C 17: 78,387,053 I303V probably benign Het
Ffar1 A T 7: 30,860,578 I298N probably benign Het
Hpx C T 7: 105,595,478 V228I probably benign Het
Igkv1-117 T G 6: 68,121,802 C112G probably damaging Het
Il3ra A G 14: 14,348,903 D99G probably benign Het
Ivl T A 3: 92,571,924 K278M probably damaging Het
Lyst A G 13: 13,687,645 T2589A probably benign Het
Madd A T 2: 91,154,448 M1359K probably damaging Het
Nav3 T C 10: 109,764,918 T1283A probably benign Het
Ncapd2 G T 6: 125,179,698 C439* probably null Het
Nebl T C 2: 17,424,522 D266G probably benign Het
Olfr1032 T G 2: 86,008,180 S135A probably damaging Het
Olfr1052 C T 2: 86,298,328 P171S probably benign Het
Olfr1062 T A 2: 86,423,307 Y123F probably damaging Het
Olfr134 T C 17: 38,175,528 V148A probably benign Het
Olfr141 T A 2: 86,806,171 Y276F probably damaging Het
Olfr1440 A G 19: 12,394,355 I31V not run Het
Olfr324 A G 11: 58,597,407 I6V unknown Het
Olfr711 C T 7: 106,972,464 probably benign Het
Olfr740 T C 14: 50,453,916 L288P possibly damaging Het
Olfr917 C T 9: 38,665,812 E11K probably benign Het
Pard3b T A 1: 62,153,989 V217E probably damaging Het
Pcdha2 T A 18: 36,939,460 I48N probably damaging Het
Pi4ka A G 16: 17,303,127 F1248L Het
Plpp4 C T 7: 129,379,477 R151C unknown Het
Pramef17 T A 4: 143,991,607 Y422F probably benign Het
Prdm16 A G 4: 154,320,882 L1245P probably damaging Het
Prob1 G A 18: 35,653,551 A550V probably benign Het
Prok1 T C 3: 107,237,092 H65R probably benign Het
Ptcd1 A G 5: 145,155,077 V404A probably benign Het
Sbf2 T C 7: 110,315,082 E1631G probably benign Het
Sdad1 C A 5: 92,300,089 K262N probably benign Het
Sh3bp1 G T 15: 78,910,072 A547S probably benign Het
Sptb T C 12: 76,628,559 D227G probably benign Het
Tbx1 A G 16: 18,588,019 M1T probably null Het
Tespa1 T A 10: 130,347,339 V51D probably damaging Het
Tmc7 T C 7: 118,566,245 N82S probably benign Het
Tmem8b A G 4: 43,689,476 D290G possibly damaging Het
Trbv13-2 A T 6: 41,121,559 T23S probably damaging Het
Trib3 A T 2: 152,338,633 D213E probably damaging Het
Tubgcp4 T C 2: 121,183,500 V178A probably benign Het
Virma T A 4: 11,539,918 C1412* probably null Het
Vmn2r108 T C 17: 20,471,500 T254A probably benign Het
Vps13d A G 4: 145,155,567 V1152A Het
Wdr47 T C 3: 108,618,968 V269A probably damaging Het
Zc3h13 T A 14: 75,324,537 D676E unknown Het
Zc3h6 T A 2: 129,017,014 S988R probably benign Het
Other mutations in Oas1f
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL02398:Oas1f APN 5 120851505 missense probably benign
R0378:Oas1f UTSW 5 120856426 missense probably damaging 0.99
R1414:Oas1f UTSW 5 120851459 intron probably benign
R1826:Oas1f UTSW 5 120855589 missense probably benign 0.33
R1848:Oas1f UTSW 5 120855429 missense probably damaging 1.00
R1895:Oas1f UTSW 5 120855585 missense probably benign 0.04
R1960:Oas1f UTSW 5 120856439 missense possibly damaging 0.54
R2193:Oas1f UTSW 5 120851585 missense probably damaging 1.00
R4622:Oas1f UTSW 5 120848327 missense probably damaging 0.98
R4758:Oas1f UTSW 5 120847480 missense probably damaging 1.00
R5882:Oas1f UTSW 5 120848253 missense probably damaging 0.99
R6515:Oas1f UTSW 5 120848434 missense probably damaging 1.00
R6944:Oas1f UTSW 5 120848184 missense probably benign 0.01
R8048:Oas1f UTSW 5 120848416 missense possibly damaging 0.91
Predicted Primers PCR Primer
(F):5'- CAGTCAGCAAACACTTCCTGG -3'
(R):5'- TTCCATCAGTCCAGTCATCCAG -3'

Sequencing Primer
(F):5'- AACACTTCCTGGCCATAAAATG -3'
(R):5'- TCAGTCCAGTCATCCAGCAGTG -3'
Posted On2020-01-23